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ACVR1(R206H) FOP mutation alters mechanosensing and tissue stiffness during heterotopic ossification
An activating bone morphogenetic proteins (BMP) type I receptor ACVR1 (ACVR1(R206H)) mutation enhances BMP pathway signaling and causes the rare genetic disorder of heterotopic (extraskeletal) bone formation fibrodysplasia ossificans progressiva. Heterotopic ossification frequently occurs following...
Autores principales: | Haupt, Julia, Stanley, Alexandra, McLeod, Claire M., Cosgrove, Brian D., Culbert, Andria L., Wang, Linda, Mourkioti, Foteini, Mauck, Robert L., Shore, Eileen M. |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
The American Society for Cell Biology
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6337906/ https://www.ncbi.nlm.nih.gov/pubmed/30379592 http://dx.doi.org/10.1091/mbc.E18-05-0311 |
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